Results 11 to 20 of about 10,664 (186)

Effectiveness and safety of canakinumab in cryopyrin-associated periodic syndrome: a retrospective study in China

open access: yesPediatric Rheumatology Online Journal
Objective Cryopyrin-associated periodic syndrome (CAPS) is characterized by excessive IL-1β release resulting in systemic and organ inflammation. As an anti-IL-1 agent, canakinumab has been approved with all CAPS phenotypes in USA and European countries.
Xiaona Zhu   +8 more
doaj   +2 more sources

CANOPY-N: A Phase 2 Study of Canakinumab or Pembrolizumab, Alone or in Combination, as Neoadjuvant Therapy in Patients With Resectable, Stage IB–IIIA NSCLC [PDF]

open access: yesJTO Clinical and Research Reports
Introduction: Canakinumab is a human monoclonal anti–interleukin-1β antibody with the potential to enhance the activity of programmed death-ligand 1 inhibitors by inhibiting protumor inflammation.
Jay M. Lee, MD   +18 more
doaj   +2 more sources

Pharmacokinetic and pharmacodynamic properties of canakinumab in patients with gouty arthritis

open access: yesJournal of Clinical Pharmacology, 2013
Pharmacokinetics and pharmacodynamics of the anti ]interleukin (IL)]1b monoclonal antibody, canakinumab, in gouty arthritis patients from three studies are reported.
Gangadhar Sunkara, Dan Howard
exaly   +2 more sources

Canakinumab for the treatment of adult-onset Still’s disease

open access: yesExpert Review of Clinical Immunology, 2020
Introduction: Adult-onset Still’s disease (AOSD) is a rare multisystem autoinflammatory disorder of unknown etiology, with clinical and biological similarities with the juvenile form (sJIA). The pivotal role of interleukin (IL)-1 gives rise to the use of
Paolo Sfriso   +2 more
exaly   +2 more sources

Long-term effectiveness and safety of canakinumab in pediatric familial Mediterranean fever patients

open access: yesModern Rheumatology, 2020
Background: Little is known about the long-term efficacy and safety of canakinumab in paediatric FMF patients. Aim: To present the single centre experience of colchicine-resistant paediatric-onset FMF patients who were treated with canakinumab by off ...
Nesrin Gülez   +2 more
exaly   +2 more sources

Canakinumab in the treatment of systemic juvenile idiopathic arthritis: a retrospective single center study in China

open access: yesFrontiers in Pediatrics
ObjectiveSystemic juvenile idiopathic arthritis (sJIA) is characterized by excessive production of proinflammatory cytokines. As an anti-IL-1 agent, canakinumab has been approved in the USA and Europe for the treatment of sJIA patients aged ≥2 years ...
Xiaona Zhu   +5 more
doaj   +2 more sources

Canakinumab and cardiovascular outcomes: results of the CANTOS trial

open access: yesJournal of Community Hospital Internal Medicine Perspectives, 2018
IL-1 cytokines are mainly responsible for controlling a series of pro-inflammatory reactions induced in response to pathogen mediated tissue injury. Among the IL-1 cytokine family, IL-1 β results in upregulation of genes responsible for boosting immune ...
Syed Raza Shah   +6 more
doaj   +2 more sources

Schnitzler syndrome refractory to anakinra: successful treatment with canakinumab

open access: yesJournal of Dermatological Treatment, 2023
Schnitzler syndrome (SchS) is a rare autoimmune and inflammatory disease mediated by interleukin-1 beta (IL-1β). Recurrent monoclonal gammopathy and chronic urticarial rash are the symptoms required for diagnosis according to the Strasbourg criteria. The
Angel Luis Salcedo-Mingoarranz   +4 more
doaj   +2 more sources

Canakinumab treatment patterns in sJIA, FMF, TRAPS, and MKD/HIDS: real-world insights from a Belgian non-interventional study [PDF]

open access: yesBMC Rheumatology
Background Canakinumab, an IL-1β inhibitor, has demonstrated long-term efficacy and safety in patients with sJIA, FMF, TRAPS, and MKD/HIDS who experience inadequate disease control with conventional treatments. This non-interventional study aimed to gain
Michel Moutschen   +10 more
doaj   +2 more sources

Neonatal-onset multisystem inflammatory disease caused by a de novo NLRP3 gene mutation: a case report and literature review [PDF]

open access: yesFrontiers in Pediatrics
BackgroundNeonatal-onset multisystem inflammatory disease (NOMID) is a rare autoinflammatory disease caused by NLRP3 mutations, leading to excessive interleukin-1β activation and potential irreversible organ damage.Case descriptionWe report a female ...
Lingxia Zhao, Lingkong Zeng, Wenhao Yuan
doaj   +2 more sources

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